"Ambry Genetics"[submitter] AND "ZNF671"[gene] - ClinVar

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2466562	NM_024833.3(ZNF671):c.1543G>A (p.Glu515Lys)	ZNF671 (E417K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197617	NM_024833.3(ZNF671):c.1357T>C (p.Cys453Arg)	ZNF671 (C355R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216213	NM_024833.3(ZNF671):c.1310G>T (p.Ser437Ile)	ZNF671 (S339I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217737	NM_024833.3(ZNF671):c.1234C>T (p.Leu412Phe)	ZNF671 (L335F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389745	NM_024833.3(ZNF671):c.1189T>C (p.Tyr397His)	ZNF671 (Y397H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259129	NM_024833.3(ZNF671):c.1106A>G (p.Tyr369Cys)	ZNF671 (Y292C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397351	NM_024833.3(ZNF671):c.1091C>T (p.Thr364Met)	ZNF671 (T364M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375829	NM_024833.3(ZNF671):c.1031G>A (p.Ser344Asn)	ZNF671 (S344N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209298	NM_024833.3(ZNF671):c.886C>T (p.Arg296Cys)	ZNF671 (R198C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215951	NM_024833.3(ZNF671):c.673G>C (p.Gly225Arg)	ZNF671 (G127R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312140	NM_024833.3(ZNF671):c.640C>T (p.Pro214Ser)	ZNF671 (P137S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239158	NM_024833.3(ZNF671):c.581G>A (p.Cys194Tyr)	ZNF671 (C194Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394032	NM_024833.3(ZNF671):c.580T>C (p.Cys194Arg)	ZNF671 (C194R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259127	NM_024833.3(ZNF671):c.550G>A (p.Gly184Arg)	ZNF671 (G184R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197622	NM_024833.3(ZNF671):c.542A>C (p.Lys181Thr)	ZNF671 (K83T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598401	NM_024833.3(ZNF671):c.505T>C (p.Cys169Arg)	ZNF671 (C71R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197621	NM_024833.3(ZNF671):c.451G>A (p.Val151Met)	ZNF671 (V53M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490116	NM_024833.3(ZNF671):c.412G>A (p.Glu138Lys)	ZNF671 (E61K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197620	NM_024833.3(ZNF671):c.399T>G (p.His133Gln)	ZNF671 (H35Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216214	NM_024833.3(ZNF671):c.336G>C (p.Gln112His)	ZNF671 (Q14H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399569	NM_024833.3(ZNF671):c.257C>T (p.Ala86Val)	ZNF671 (A86V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3197619	NM_024833.3(ZNF671):c.227A>T (p.Asp76Val)	ZNF671 (D76V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2367116	NM_024833.3(ZNF671):c.125C>G (p.Thr42Arg)	ZNF671 (T42R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3197615	NM_024833.3(ZNF671):c.100G>C (p.Ala34Pro)	ZNF671 (A34P)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2288064	NM_024833.3(ZNF671):c.94G>A (p.Val32Ile)	ZNF671 (V32I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2488688	NM_024833.3(ZNF671):c.68C>T (p.Ser23Leu)	ZNF671 (S23L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3259128	NM_024833.3(ZNF671):c.62C>T (p.Pro21Leu)	ZNF671 (P21L)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2494336	NM_024833.3(ZNF671):c.61C>T (p.Pro21Ser)	ZNF671 (P21S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2527434	NM_024833.3(ZNF671):c.52T>C (p.Cys18Arg)	ZNF671 (C18R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3197618	NM_024833.3(ZNF671):c.17C>T (p.Ser6Phe)	ZNF671 (S6F)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance

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Items: 30